Structural determinants of Ca2+ permeability and conduction in the human 5-hydroxytryptamine type 3A receptor.
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Novel structural determinants of single channel conductance and ion selectivity in 5-hydroxytryptamine type 3 and nicotinic acetylcholine receptorsPathways and Barriers for Ion Translocation through the 5-HT3A Receptor ChannelLength and amino acid sequence of peptides substituted for the 5-HT3A receptor M3M4 loop may affect channel expression and desensitizationEvidence for α-helices in the large intracellular domain mediating modulation of the α1-glycine receptor by ethanol and Gβγ.Therapeutics of 5-HT3 receptor antagonists: current uses and future directions.Discrete M3-M4 intracellular loop subdomains control specific aspects of γ-aminobutyric acid type A receptor function.The basic property of Lys385 is important for potentiation of the human α1 glycine receptor by ethanol.The 5-HT3B subunit affects high-potency inhibition of 5-HT3 receptors by morphinePermeation properties of the hair cell mechanotransducer channel provide insight into its molecular structure5-HT(3) receptors.The minimum M3-M4 loop length of neurotransmitter-activated pentameric receptors is critical for the structural integrity of cytoplasmic portals.Calcium modulation of 5-HT3 receptor binding and function.The 5-HT3AB receptor shows an A3B2 stoichiometry at the plasma membrane.Mutagenic analysis of the intracellular portals of the human 5-HT3A receptor.Single-channel kinetic analysis for activation and desensitization of homomeric 5-HT(3)A receptors.Copper and protons directly activate the zinc-activated channelThe auspicious role of the 5-HT3 receptor in depression: a probable neuronal target?The structural basis of function in Cys-loop receptors.The structural mechanism of the Cys-loop receptor desensitization.Discriminating between 5-HT₃A and 5-HT₃AB receptorsRings of charge within the extracellular vestibule influence ion permeation of the 5-HT3A receptor.Characterization of the effects of charged residues in the intracellular loop on ion permeation in alpha1 glycine receptor channels.A novel mechanism of modulation of 5-HT₃A receptors by hydrocortisone.Agonists and antagonists induce different palonosetron dissociation rates in 5-HT₃A and 5-HT₃AB receptors.Novel regulatory site within the TM3-4 loop of human recombinant alpha3 glycine receptors determines channel gating and domain structure.Structural principles of distinct assemblies of the human α4β2 nicotinic receptor.
P2860
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P2860
Structural determinants of Ca2+ permeability and conduction in the human 5-hydroxytryptamine type 3A receptor.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@en
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@nl
type
label
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@en
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@nl
prefLabel
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@en
Structural determinants of Ca2 ...... xytryptamine type 3A receptor.
@nl
P2093
P2860
P356
P1476
Structural determinants of Ca2 ...... oxytryptamine type 3A receptor
@en
P2093
Janna Kozuska
Jeremy J Lambert
John A Peters
Matthew R Livesey
Michelle A Cooper
Tarek Z Deeb
P2860
P304
19301-19313
P356
10.1074/JBC.M802406200
P407
P577
2008-05-12T00:00:00Z